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So I'm trying to figure out where the disconnect happens between Medicaid and the patient. I'm sure we've all seen or heard of the recent article where a family, who had been receiving Medicaid/Medicare benefits was living in a million dollar beach house. Then I see the patient angry because their Caresource card was rejected and we had to rebill under Advance PCS of Texas... and they almost had to pay cash for their non-life sustaining medication aka <insert ADHD med here>..... and they speed off in their Escalade/Lexus/various other $50,000+ gas guzzler vehicle.
Then you've got my little brother who was diagnosed with DM type 1 when he was 28 years old after going into DKA with no family history of DM. He can't afford to pay for his insulin because he gets no insurance through his part time job and lives in a small town trying to get his culinary degree and is denied for financial assistance.
So what gives? How are some individuals able to get their amphetamine Rx's and everything else for free, including OTC meds and drive expensive cars.. yet people actually in need are denied? Where's the disconnect?
Then you've got my little brother who was diagnosed with DM type 1 when he was 28 years old after going into DKA with no family history of DM. He can't afford to pay for his insulin because he gets no insurance through his part time job and lives in a small town trying to get his culinary degree and is denied for financial assistance.
So what gives? How are some individuals able to get their amphetamine Rx's and everything else for free, including OTC meds and drive expensive cars.. yet people actually in need are denied? Where's the disconnect?